Relative importance of nitrite oxidation by hypochlorous acid under chloramination conditions

Nitrification can occur in water distribution systems where chloramines are used as the disinfectant. The resulting product, nitrite, can be oxidized by monochloramine and hypochlorous acid (HOCl), potentially leading to rapid monochloramine loss. This research characterizes the importance of the HOCl reaction, which has typically been ignored because of HOCl's low concentration. Also, the general acid-assisted rate constants for carbonic acid and bicarbonate ion were estimated for the monochloramine reaction. The nitrite oxidation reactions were incorporated into a widely accepted chloramine autodecomposition model, providing a comprehensive model that was implemented in AQUASIM. Batch kinetic experiments were conducted to evaluate the significance of the HOCl reaction and to estimate carbonate buffer rate constants for the monochloramine reaction. The experimental data and model simulations indicated that HOCl may be responsible for up to 60% of the nitrite oxidation, and that the relative importance of the HOCl reaction for typical chloramination conditions peaks between pH 7.5 and 8.5, generally increasing with (1) decreasing nitrite concentration, (2) increasing chlorine to nitrogen mass ratio, and (3) decreasing monochloramine concentration. Therefore, nitrite's reaction with HOCl may be important during chloramination and should be included in water quality models to simulate nitrite and monochloramine's fate.     

Chlorine and carbon isotopes fractionation during volatilization and diffusive transport of trichloroethene in the unsaturated zone

To apply compound-specific isotope methods to the evaluation of the origin and fate of organic contaminants in the unsaturated subsurface, the effect of physicochemical processes on isotope ratios needs to be known. The main objective of this study is to quantify chlorine and carbon isotope fractionation during NAPL-vapor equilibration, air-water partitioning, and diffusion of trichloroethene (TCE) and combinations of these effects during vaporization in porous media. Isotope fractionation is larger during NAPL-vapor equilibration than air-water partitioning. During NAPL-vapor equilibration, carbon, and chlorine isotope ratios evolve in opposite directions although both elements are present in the same bond, with a normal isotope effect for chlorine (ε(Cl) = -0.39 ± 0.03‰) and an inverse effect for carbon (ε(C) = +0.75 ± 0.04‰). During diffusion-controlled vaporization in a sand column, no significant carbon isotope fractionation is observed (ε(C) = +0.10 ± 0.05‰), whereas fairly strong chlorine isotope fractionation occurs (ε(Cl) = -1.39 ± 0.06‰) considering the molecular weight of TCE. In case of carbon, the inverse isotope fractionation associated with NAPL-vapor equilibration and normal diffusion isotope fractionation cancel, whereas for chlorine both processes are accompanied by normal isotope fractionation and hence they cumulate. A source of contamination that aged might thus show a shift toward heavier chlorine isotope ratios.     

Using a passive multilayer sampler for measuring detailed profiles of gas-phase VOCs in the unsaturated zone

The purpose of this study was to test in the laboratory the performance of a passive multilayer sampler (MLS) for obtaining detailed profiles of gas-phase volatile organic compounds (VOCs) in unsaturated sediments. The MLS is essentially a chain of isolated, cylindrical stainless steel dialysis cells filled with distilled water and closed with membranes at both ends. The sampling principle is based on passive equilibration of the unsaturated zone gas phase with water in the cells. Using trichloroethene (TCE) as a model VOC, and after testing the required equilibration time in the laboratory (about 50 h), results of a large container (210 L) experiment show that TCE concentrations obtained by the MLS deployed inside a well screen corresponded very well to the profile obtained by dialysis cells buried in the sediment. A field profile taken at the saturated-unsaturated interface region of a VOC-contaminated area using the MLS shows steep TCE concentration gradients (1119 microg TCE/L-air/cm) in the gas phase of the unsaturated zone just above the water table.     

Characterization of the polarity of natural organic matter under ambient conditions by the polarity rapid assessment method (PRAM)

The polarity rapid assessment method (PRAM) characterizes the polarity of aqueous natural organic matter (NOM) by quantifying the amount of material adsorbed onto different solid-phase extraction (SPE) sorbents. The analysis is performed under ambient conditions resulting in the elimination of pretreatment steps that may alterthe chemical characteristics of the NOM, allowing an accurate representation of its polarity as it exists in the environment. Additionally, analysis only requires 200 mL of sample and can be performed in 2 h. In this paper, the underlying theory of the method is presented, followed by its optimization, with emphasis on the development of conditions for the analysis of NOM in natural waters. A series of organic probe compounds showed that the most important physicochemical property describing the interaction between the NOM and the SPE sorbents was the hydrophobic surface area, allowing for the estimation of the hydrophobic character under ambient conditions. Evaluation of the effects of chemical concentration, pH, and ionic strength show that (1) concentration did not have an effect on PRAM characterization as long as the pH and ionic strength remained constant; (2) changes in pH and ionic strength resulted in considerable changes in PRAM characterization, as a result of the changes in configuration of the NOM; and (3) PRAM characterization of NOM can be completed in the concentration range of < 10 mg C/L, although this range could be expanded by evaluating the effect of concentration on a site-specific basis. Results indicate that measurement of both ultraviolet absorption and dissolved organic carbon show complementary results as they measure different aspects of NOM.     

Dissolution of technetium(IV) oxide by natural and synthetic organic ligands under both reducing and oxidizing conditions

Technetium-99 (Tc) in nuclear waste is a significant environmental concern due to its long half-life and high mobility in the subsurface. Reductive precipitation of technetium(IV) oxides [TcO(2)(s)] is an effective means of immobilizing Tc, thereby impeding its migration in groundwater. However, technetium(IV) oxides are subject to dissolution by oxidants and/or complexing agents. In this study we ascertain the effects of a synthetic organic ligand, ethylenediaminetetraacetate (EDTA), and two natural humic isolates on the dissolution and solubility of technetium(IV) oxides. Pure synthetic technetium(IV) oxide (0.23 mM) was used in batch experiments to determine dissolution kinetics at pH ～6 under both reducing and oxidizing conditions. All organic ligands were found to enhance the dissolution of technetium(IV) oxides, increasing their solubility from ～10(-8) M (without ligands) to 4 × 10(-7) M under strictly anoxic conditions. Reduced Tc(IV) was also found to reoxidize rapidly under oxic conditions, with an observed oxidative dissolution rate approximately an order of magnitude higher than that of ligand-promoted dissolution under reducing conditions. Significantly, oxidative dissolution was inhibited by EDTA but enhanced by humic acid compared to experiments without any complexing agents. The redox functional properties of humics, capable of facilitating intramolecular electron transfer, may account for this increased oxidation rate under oxic conditions. Our results highlight the importance of complex interactions for the stability and mobility of Tc and thus for the long-term fate of Tc in contaminated environments.     

Virus retention and transport in chemically heterogeneous porous media under saturated and unsaturated flow conditions

Retention and transport of colloids and microorganisms are complex processes, especially in the vadose zone due to the more complicated water flow regime and additional interfacial reactions involved. In this study, we examined the retention and transport behavior of two bacteriophages, MS-2 and phiX174, in homogeneous and chemically heterogeneous media under variably saturated conditions. Column experiments with glass beads (treated to have either hydrophilic or hydrophobic surface properties) were conducted using a phosphate-buffered saline solution at different pore water ionic strengths ranging from 0.025 to 0.163 M. In columns packed with 100% hydrophilic glass beads, retention of the viruses increased with decreasing water content and increasing ionic strength, a result similar to those reported in the literature. However, greater retention of both MS-2 and phiX174 was observed in saturated columns than in unsaturated columns packed with a 1:1 mixture of hydrophilic and hydrophobic glass beads, especially at high ionic strengths. This result contradicts the common belief that viruses (and colloids in general) are subject to greater removal in unsaturated media. Our study suggests that while the mechanisms controlling colloid interfacial interactions (i.e., attachment on solid-water and air-water interfaces and film straining) on the pore scale are relevant, nonuniform wetting conditions due to heterogeneous grain surface hydrophobicity can strongly influence water flow and phase interconnection. Under these conditions, hydrodynamic effects on the mesopore scale will dominate pore-scale interfacial reactions in controlling the extent of colloid retention and movement in unsaturated media.     

Recommended food supplies under conditions of natural and provoked catastrophes

Natural catastrophes include those of biological origin as the pandemic provoked by virus SARS CoV2, earthquakes, flooding and hurricanes among others, while provoked ones are mainly those related to wars and social movements. These situations may cause food shortage and challenge food safety and security systems. In this review, strategies to produce foods aimed to alleviate food needs before, during and after catastrophic conditions are described based on the supply of various processed, intermediate and low moisture foods and three categories of food supplies are depicted based on the nature of the adverse conditions, Also, relevant patents on on innovative food preparations and containers for disaster areas are discussed. Innovation to produce appropriate and nutritious foods for disaster zones may include food bags containing individual packages of high protein, high fiber/vitamins and carbohydrate/oils ingredients in dried/vitreous state. Additionally, the role of food structure on food preservation is mentioned in the context of ready to eat, nutritious and sensory acceptable food supplies during natural or provoked catastrophes is also reported.     

Enhancement of cometabolic biodegradation of trichloroethylene (TCE) gas in biofiltration

A biofilter column inoculated with Pseudomonas putida F1 was operated to study cometabolic biodegradation of trichloroethylene (TCE) gas using toluene as a primary substrate. Variations in the efficiency and capacity of TCE elimination with different inlet concentrations of toluene and TCE were investigated in order to understand the competitive inhibition between toluene and TCE. Two toluene feeding methods, stage feeding along the column and cyclic feeding, were examined as strategies to enhance TCE cometabolic biodegradation by avoiding the toluene inhibition of TCE biodegradation and the toxic effect of TCE on cells and toluene dioxygenase enzymes. It was concluded that both methods are promising and that the determination of a suitable feeding frequency, recovery period, and inlet toluene concentration was required to optimize cyclic feeding in the cometabolic biodegradation of TCE.     

Slaughter value and flesh characteristics of European catfish (Silurus glanis) fed natural and formulated feed under different rearing conditions

The experimental material was comprised of European catfish (Silurus glanis) individuals aged 2.5 years that were reared on natural feed in earthen ponds and individuals aged 1.5 years cultivated intensively on formulated feed in recirculating systems. Weight gain and morphometric parameters were measured along with physical and color characteristics and proximate composition of fillets. Despite the different age and diets of the fish, no differences were observed in the linear biometric indices. The total weight of the fish of both groups and their condition coefficients were also similar. In addition, no differences were reported in their body weight or head and gutted (H&G) carcass and fillet yields. Proximate composition analysis demonstrated a lack of differences in the contents of dry matter. Of the dry matter, differences were reported in the fat content, which was higher in the catfish fed formulated feed. The color of the fillets was characterized by high values of lightness, negative values of redness, and positive values of yellowness, and the fish fed formulated feed displayed higher saturation of green. The flesh of both groups of catfish demonstrated similar pH values and water retention capacity, whereas the values of thermal drip appeared to be higher in the fish fed formulated feed.     

Comparison of some components of pigs kept in natural (free-range) and large-scale conditions

A new pig genotype of Hungarian Large White (75%) × Mangalica (pig with curly bristles, 25%) was used in the experiments. The experimental group was kept in a farming system under strictly natural circumstances until a body weight of 120 kg was attained. Neither antibiotics nor yield-increasing hormones were given to this group. The control group was kept in the usual large-scale farming conditions until body weight of 120 kg was attained. In most cases, protein, zinc, and copper levels and, in some cases, iron levels were significantly higher in some major cuts (neck-end (Boston-butt), loin, ham) of the 'free-range' pigs (n = 12) in comparison with the control animals kept in large-scale farming conditions. There was, on average, 15% less cholesterol in the muscles and 30% less cholesterol in the liver and less linoleic acid in all tissues of 'free-range' pigs than in the control group. There was less fat, but the amount of thiamin and riboflavin in the liver of the naturally kept pigs was twice that in the controls. In respect of TBA-reactive compounds, there were no significant differences between the two groups, but superoxide dismutase (SOD) showed significantly higher activities in all cuts from pigs kept in a large-scale farming system. This may be the effect of a higher level of linoleic acid in the fat.     

Seasonal variability and long term trends of chlorofluorocarbon mixing ratios in the unsaturated zone

To investigate processes that might affect chlorofluorocarbon (CFC) mixing ratios at the water table, a time series was obtained of unsaturated zone soil gas CFCs to depths of ca. 4 m at a site near New York City (NYC). Observed CFC 11, 12, and 113 mixing ratios were lower in winter than expected from either a local, high-resolution time series or remote atmospheric mixing ratios. A diffusion model, which includes seasonal changes in soil temperature, moisture, and CFC solubility, reproduces to first order the observed soil gas mixing ratios for CFC 11 and 12. Underestimation by the model of the seasonal cycle of CFC 11 points to changing levels of sorption to soils due to seasonal changes in temperature as an additional cause of the cycle seen in CFC 11 mixing ratios in soil air. In the case of spring recharge, low CFC mixing ratios in soil air caused by increased solubility may result in low CFC 11 concentrations in groundwater and, when dating groundwater recharged before the 1990s with CFCs, older apparent ages by up to 4 years. Attempts to observe average atmospheric CFC levels from soil gas are also significantly hindered by these seasonal fluctuations. Our results indicate the importance of considering seasonal changes in soil temperature when making precise observations of even very moderately soluble gases in the unsaturated zone and shallow groundwater.     

Widespread natural perchlorate in unsaturated zones of the southwest United States

A substantial reservoir (up to 1 kg ha(-1)) of natural perchlorate is present in diverse unsaturated zones of the arid and semi-arid southwestern United States. The perchlorate co-occurs with meteoric chloride that has accumulated in these soils throughout the Holocene [0 to 10-15 ka (thousand years ago)] and possibly longer periods. Previously, natural perchlorate widely believed to be limited to the Atacama Desert, now appears widespread in steppe-to-desert ecoregions. The perchlorate reservoir becomes sufficiently large to affect groundwater when recharge from irrigation or climate change flushes accumulated salts from the unsaturated zone. This new source may help explain increasing reports of perchlorate in dry region agricultural products and should be considered when evaluating overall source contributions.     

太阳能干燥对干湿梅品质的影响

以干湿梅为样品,利用小型太阳能连续干燥设备,研究了干湿梅的干燥特性,分析了产品的理化性质和感官品质。结果表明,干燥过程中干燥介质的温湿度与外界环境相比有明显差异,干燥室白天日照时温度会高于环境温度,干燥时间明显缩短,高效且避免了缓苏产品色泽口感品质的不利影响;干燥过程是内部水分扩散控制的降速干燥过程,达到目标湿基湿含量(58%～60%)和盐含量(28%～32%)时,自然日晒干燥约需50h,而太阳能自然对流干燥只需14h;水分扩散速率和理化指标随样品在干燥室中所处位置不同而异,环境温度的上升使其在干燥7～10h中有较高的干燥速率;干燥过程中样品的色泽会逐渐变深、体积略有收缩、果肉硬度增加,实验表明在干燥室第二层的样品感官分值为4.40±0.03,整体感官品质优于自然日晒干燥产品。     

Photolysis studies of technical decabromodiphenyl ether (DecaBDE) and ethane (DeBDethane) in plastics under natural sunlight

Photodebromination of technical decabromodiphenyl ether (DecaBDE) incorporated into high-impact polystyrene (HIPS) and TV casings was compared under natural sunlight conditions with that of technical decabromodiphenyl ethane (DeBDethane). BDE 209 in pulverized HIPS+DecaBDE samples degraded with a half-life of 51 days. In contrast, no marked loss of DeBDethane occurred throughout the experimental period of 224 days. During BDE 209 photolysis in HIPS+DecaBDE samples, partly debromination to nona- and octa-BDE was observed, however, environmentally relevant polybrominated diphenyl ether (PBDE) congeners such as BDE 47, 99, and 100 were not formed. Formation of polybrominated dibenzofurans (PBDFs) was clearly apparent in the flame-retarded plastics that we investigated. In the HIPS+DecaBDE samples, the PBDF concentration increased by about 40 times after 1 week of exposure, with a concomitant decrease in BDE 209. In the TV casing, tetra- to octa-BDF congener concentrations increased continuously during the experiment Although the concentrations of PBDFs found in the plastic matrices tested were 1 to 4 orders of magnitude lower than those of PBDEs, more attention should be paid to the fact that PBDFs are formed by sunlight exposure during normal use as well as disposal/recycling processes of flame-retarded consumer products.     

Retention and transport of amphiphilic colloids under unsaturated flow conditions: effect of particle size and surface property

The purpose of this study was to examine the mechanisms responsible for deposition and transport of amphiphilic colloids with a wide range of particle sizes (20-420 nm) through porous media. A series of saturated and unsaturated column experiments were conducted using amphiphilic latex microspheres and a hydrophilic silica colloid. We found that the amphiphilic latex particles were retained to a greater extentthan the hydrophilic silica colloid in unsaturated media. This was attributed to colloidal attachment atthe air-water interface due mainly to hydrophobic interactions. We also found that dependence of colloid retention on particle size was nonlinear. There existed a fraction of colloids with greater mobility than other fractions, which we referred to as the most mobile colloids. As particle size increased from 20 to 420 nm, colloid deposition rate first decreased to reach a minimum value at --100 nm then increased, indicating that different retention mechanisms were involved. We showed that conducting saturated transport experiments and analysis using filtration theory may be an effective approach for determining the most mobile colloid size(s) in porous media, perhaps even for unsaturated flow conditions. This study highlights the importance of including size effect and surface properties when predicting concentrations and fluxes of amphiphilic colloids or colloid-bound amphiphilic and hydrophobic contaminants in the subsurface environment.     

In situ colloid mobilization in Hanford sediments under unsaturated transient flow conditions: effect of irrigation pattern

Colloid transport may facilitate off-site transport of radioactive wastes at the Hanford site, Washington State. In this study, column experiments were conducted to examine the effect of irrigation schedule on releases of in situ colloids from two Hanford sediments during saturated and unsaturated transientflow and its dependence on solution ionic strength, irrigation rate, and sediment texture. Results show that transient flow mobilized more colloids than steady-state flow. The number of short-term hydrological pulses was more important than total irrigation volume for increasing the amount of mobilized colloids. This effect increased with decreasing ionic strength. At an irrigation rate equal to 5% of the saturated hydraulic conductivity, a transient multipulse flow in 100 mM NaNO3 was equivalent to a 50-fold reduction of ionic strength (from 100 mM to 2 mM) with a single-pulse flow in terms of their positive effects on colloid mobilization. Irrigation rate was more important for the initial release of colloids. In addition to water velocity, mechanical straining of colloids was partly responsible for the smaller colloid mobilization in the fine than in the coarse sands, although the fine sand contained much larger concentrations of colloids than the coarse sand.     

Reoxidation of reduced uranium with iron(III) (hydr)oxides under sulfate-reducing conditions

In cultures of Desulfovibrio desulfuricans 620 the effects of iron(III) (hydr)oxides (hematite, goethite, and ferrihydrite) on microbial reduction and reoxidation of uranium (U) were evaluated under lactate-limited sulfate-reducing conditions. With lactate present, G20 reduced U(VI) in both 1,4-piperazinediethanesulfonate (PIPES) and bicarbonate buffer. Once lactate was depleted, however, microbially reduced U served as an electron donor to reduce Fe(III) present in iron(III) (hydr)oxides. With the same initial amount of Fe(III) (10 mmol/L) for each iron(III) (hydr)oxide, reoxidation of U(IV) was greater with hematite than with goethite orferrihydrite. As the initial mass loading of hematite increased from 0 to 20 mmol of Fe(III)/L, the rate and extent of U(IV) reoxidation increased. Subsequent addition of hematite [15 mmol of Fe(III)/L] to stationary-phase cultures containing microbially reduced U(IV) also resulted in rapid reoxidation to U(VI). Analysis by U L3-edge X-ray absorption near-edge spectroscopy (XANES) of microbially reduced U particles yielded spectra similar to that of natural uraninite. Observations by high-resolution transmission electron microscopy, selected area electron diffraction, and energy-dispersive X-ray spectroscopic analysis confirmed that precipitated U associated with cells was uraninite with particle diameters of 3-5 nm. By the same techniques, iron sulfide precipitates were found to have a variable Fe and S stoichiometry and were not associated with cells.     

Relative importance of pre-partum and post-partum factors in the control of milk yield in the guinea-pig

Examination of data pertaining to milk yield and litter growth rate of guinea-pigs at peak lactation showed that milk yield increased with increasing number of pups carried by the dam during pregnancy and also with increasing maternal weight. There was a significant linear correlation (P less than 0.05) of mammary gland weight (expressed per unit of maternal body weight) with litter size. Increasing litter size, within 18 h of parturition, from 1 pup to 5 pups did not elicit a response in milk yield. Decreasing litter size from 5 pups to 1 pup reduced milk yield to the level expected of a monotocous dam. Data are presented showing the ability of the guinea-pig pup to survive from birth without access to milk and the inadequacy of milk supply to meet litter requirements when the litter size is more than 2 pups. The mechanisms controlling lactation in the guinea-pig are discussed in relation to data obtained in other species.     

Evaluation of a chlorous acid-chlorine dioxide teat dip under experimental and natural exposure conditions

A postmilking teat dip containing chlorous acid-chlorine dioxide was evaluated by experimental challenge and in two herds under natural exposure. The test product had an efficacy of 78.9% against Staphylococcus aureus and 52.5% against Streptococcus agalactiae in the experimental challenge trial. The product was compared with a 1% iodine product in a 15-mo natural exposure study. Post-dipping with chlorous acid-chlorine dioxide reduced incidence of udder infection by major mastitis pathogens 36.1% when data were combined from the two herds. The 1% iodine and the chlorous acid-chlorine dioxide products were not equivalent for major mastitis pathogens; the test product was more effective. Incidence of udder infection by environmental mastitis pathogens was reduced 36.8% in both herds combined. Efficacy of the two teat dips was equivalent for environmental pathogens.